A python script to explain the results of the PREDIPATH output file
Some examples of output:
A nice example: a true pathogenic genome
Another nice example: a true non pathogenic genome
Nearly a pathogenic genome
Nearly a non pathogenic genome
A possible case: not enough found markers to decide
An example with three classes
You can download the script here and its included file there. The archive is Python_output2html.zip.
Here is its contents:
Retour à la page principale de (gH)